A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568240



Internal ID20941311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85194538..85195370hg38UCSC Ensembl
chr8:86106773..86107605hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278900
Samples
Known GenesE2F5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568240
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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